ClinVar Miner

Submissions for variant NM_002180.2(IGHMBP2):c.1418+18A>G (rs112575423)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000249077 SCV000308709 benign not specified criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173362 SCV001336450 benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
GeneDx RCV001668478 SCV001890802 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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